Esters of prostacyclin-type compounds

ABSTRACT

Acyl-substituted phenyl esters of prostacyclin-type compounds, for example the 4-acetylphenyl ester of prostacyclin (PGI 2 ) illustrated by the formula ##STR1## and including esters of the isomeric 6-hydroxy-PGI 1  and 6-keto-PGF 1 α compounds, said esters having pharmacological activity. Processes for preparing them and the appropriate intermediates are disclosed.

The present application is a divisional application of Ser. No. 933,329, filed Aug. 14, 1978, now issued as U.S. Pat. No. 4,180,657, on Dec. 25, 1979.

The present invention relates to prostaglandin analogs for which the essential material constituting a disclosure therefor is incorporated by reference here from U.S. Pat. No. 4,180,657, issued Dec. 25, 1979. 

I claim:
 1. An acid ester of a 6a-carba prostacyclin analog of the formula ##STR2## wherein L₁ is (1) --(CH_(z))_(n) -- wherein n is one to 5, inclusive,(2) --(CH₂)_(p) --CF₂ -- wherein p is 2, 3, or 4, or (3) --(CH₂)_(v) --CH═CH-- wherein v is 1, 2, or 3, wherein M₃ is ##STR3## wherein Q is ##STR4## wherein R₄ is hydrogen or alkyl of one to 4 carbon atoms, inclusive, wherein R₁ is alkyl of one to 4 carbon atoms with the proviso that when R₁ is tert-butyl the group ##STR5## is in the 4-position, wherein R₃ is ##STR6## wherein C_(g) H₂.sbsb.g is alkylene of one to 9 carbon atoms, inclusive, with one to 5 carbon atoms, inclusive, in the chain between --CR₅ R₆ -- and terminal methyl, wherein R₅ and R₆ are hydrogen, alkyl of one to 4 carbon atoms, inclusive, or fluoro, being the same or different, with the proviso that one of R₅ and R₆ is fluoro only when the other is hydrogen or fluoro; wherein R₁₂ is ##STR7## wherein X is (1) trans-CH═CH--(2) cis-CH═CH-- (3) --C.tbd.C-- or (4) --CH₂ CH₂ --.
 2. (5Z and 5E)-6a- Carba-PGI₂, 4-acetylphenyl ester, compounds according to claim
 1. 